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Compound A has the formula C H and is known not to contain any triple 10"16 ponds. When treated with excess hydrogen and a platinum catalyst, Compoun A is converted to compound B with the formula CH„. Compound B can be 10 22 dentified as 2,6-dimethyloctane. Ozonolysis of compound A followed by reatment with Zn and H,0 yields 2 mol of formaldehyde (HCHO), 1 mol of cetone (CH̟COCH), and compound C with the formula C̟H_0̟.

Compound A has the formula C H and is known not to contain any triple 10"16 ponds. When treated with excess hydrogen and a platinum catalyst, Compoun A is converted to compound B with the formula CH„. Compound B can be 10 22 dentified as 2,6-dimethyloctane. Ozonolysis of compound A followed by reatment with Zn and H,0 yields 2 mol of formaldehyde (HCHO), 1 mol of cetone (CH̟COCH), and compound C with the formula C̟H_0̟.

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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[VII4,5] Instructions: Answer the following: (Refer to the photo below)

4. What is the structure of compound C?

5. What is the structure of compound A?

Compound A has the formula C„H and is known not to contain any triple 10 16 bonds. When treated with excess hydrogen and a platinum catalyst, Compound A is converted to compound B with the formula CH,„: Compound B can be identified as 2,6-dimethyloctane. Ozonolysis of compound A followed by treatment with Zn and H,0 yields 2 mol of formaldehyde (HCHO), 1 mol of acetone (CH COCH,), and compound C with the formula C,H,0,.
Transcribed Image Text:Compound A has the formula C„H and is known not to contain any triple 10 16 bonds. When treated with excess hydrogen and a platinum catalyst, Compound A is converted to compound B with the formula CH,„: Compound B can be identified as 2,6-dimethyloctane. Ozonolysis of compound A followed by treatment with Zn and H,0 yields 2 mol of formaldehyde (HCHO), 1 mol of acetone (CH COCH,), and compound C with the formula C,H,0,.
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